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FDA 510(k)

LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP

K-Number: K913616 · 1991-11-07

ApplicantImplant Technology, Inc.
Decision Date1991-11-07
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP is the device name listed in this FDA 510(k) record. The listed applicant is Implant Technology, Inc.. It received FDA 510(k) clearance on 1991-11-07 under 510(k) number K913616. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP?

LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP is a medical device that received FDA 510(k) clearance on 1991-11-07. The listed applicant is Implant Technology, Inc.. The 510(k) number is K913616.

When did LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP receive FDA 510(k) clearance?

LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP received FDA 510(k) clearance on 1991-11-07, under 510(k) number K913616.

Who is the listed applicant for LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP?

The FDA 510(k) record lists Implant Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP?

The FDA product code for LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP is JDI.

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Other records listing Implant Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K921525HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESISK915617LSF HA COATED FEMORAL HIPK920021LSF TOTAL HIP SYSTEM - MULLER-TYPE ACETABULAR CUPK902727LSF CEMENTED FEMORAL HIPK901460LSF(TM) TOTAL HIP SYSTEMK891472IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR

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Related Devices (Code: JDI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253515Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and AugmentsBiomet Orthopedics, Inc.K253434OSSTM Orthopedic Salvage SystemBiomet, Inc.K243571Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained LinersZimmer BiometK240783Anthology Hip Stems; CPCS Hip Stems; Femoral Heads; R3 Acetabular Liners; Spectron Hip Stems; Synergy Hip StemsSmith & Nephew, Inc.K241716Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee ComponentHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK240418Stryker Orthopaedics Hip Systems Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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